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Decentralized Clinical Trials Manager Jobs (NOW HIRING)

As a Principal Clinical System Lead, working as a Decentralized Clinical Trials Lead exclusively ... Clinical Supplies, Biostatistics, Vendor Management, Procurement) in the sourcing, evaluation and ...

As a Clinical Trials Manager at Gilead/Kite, you will be responsible for: * Coordinating and supervising all aspects of a clinical study. Monitors clinical trial sites. * Assists Clinical Program ...

As a Clinical Trials Manager at Gilead/Kite, you will be responsible for: * Coordinating and supervising all aspects of a clinical study. Monitors clinical trial sites. * Assists Clinical Program ...

As a Clinical Trials Manager at Gilead/Kite, you will be responsible for: * Coordinating and supervising all aspects of a clinical study. Monitors clinical trial sites. * Assists Clinical Program ...

The Manager Clinical Trials position monitors progress and performance of all projects to include quality of services, timelines, financial viability, compliance with federal, state and/or other ...

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Decentralized Clinical Trials Manager information

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How much do decentralized clinical trials manager jobs pay per hour?

As of Jul 29, 2026, the average hourly pay for decentralized clinical trials manager in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What are some common challenges faced by a Decentralized Clinical Trials Manager, and how can they be addressed?

A Decentralized Clinical Trials Manager often encounters challenges related to coordinating remote sites, ensuring data quality, and maintaining effective communication among dispersed teams and participants. Addressing these issues requires robust digital platforms for data collection, clear standardized procedures, and regular virtual touchpoints with all stakeholders. Building strong relationships with site coordinators and providing thorough training on decentralized protocols also helps mitigate potential barriers and ensures trial integrity.

What is the difference between Decentralized Clinical Trials Manager vs Clinical Trial Coordinator?

AspectDecentralized Clinical Trials ManagerClinical Trial Coordinator
ResponsibilitiesOversees decentralized trial operations, manages remote sites, ensures compliance across multiple locationsAssists with trial logistics, coordinates site activities, and supports data collection
Required CredentialsBachelor's degree in life sciences, clinical research experience, knowledge of decentralized trial technologiesBachelor's degree, clinical research training, familiarity with trial procedures
Work EnvironmentRemote and on-site, collaborating with multiple decentralized sitesPrimarily on-site or office-based at trial sites or research centers
Industry UsageGrowing in decentralized and virtual trial settingsTraditional clinical trial settings

The Decentralized Clinical Trials Manager focuses on managing remote and decentralized trial operations, while the Clinical Trial Coordinator handles day-to-day site activities. Both roles require clinical research knowledge, but the manager's role is broader, overseeing multiple sites and remote technologies.

What does a Decentralized Clinical Trials Manager do?

A Decentralized Clinical Trials Manager oversees the planning, implementation, and management of clinical trials that use digital technologies to remotely monitor and collect data from participants. This role involves coordinating virtual and hybrid trial operations, ensuring regulatory compliance, and working with various stakeholders, such as investigators, technology vendors, and sponsors. The manager is responsible for ensuring participant safety, data integrity, and efficient execution of decentralized trial processes, often utilizing telemedicine, wearables, and electronic data capture systems.

What are the key skills and qualifications needed to thrive as a Decentralized Clinical Trials Manager, and why are they important?

To excel as a Decentralized Clinical Trials Manager, you need expertise in clinical trial operations, regulatory compliance, and project management, often supported by a degree in life sciences or related field. Familiarity with digital health technologies, remote monitoring platforms, and electronic data capture (EDC) systems is crucial, along with certifications like GCP (Good Clinical Practice). Excellent communication, problem-solving, and adaptability help manage cross-functional teams and rapidly changing trial environments. These skills ensure effective coordination, data integrity, and patient engagement in decentralized clinical research.
More about Decentralized Clinical Trials Manager jobs
What cities are hiring for Decentralized Clinical Trials Manager jobs? Cities with the most Decentralized Clinical Trials Manager job openings:
What states have the most Decentralized Clinical Trials Manager jobs? States with the most job openings for Decentralized Clinical Trials Manager jobs include:
Infographic showing various Decentralized Clinical Trials Manager job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Decentralized Clinical Trials Lead

410 ICR United States USA

Blue Bell, PA โ€ข On-site

Full-time

Posted yesterday


Job description

DCT Lead

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Principal Clinical System Lead, working as a Decentralized Clinical Trials Lead exclusively assigned and embedded within a Pharmaceutical Company, you will provide strategic leadership and direction in the design, development, and implementation of eCOA (electronic Clinical Outcome Assessment) clinical systems and technologies.

What You Will Do:

You will support the Sponsorโ€™s eCOA clinical systems, taking a leadership role in eCOA project implementation, ensuring that deliverables meet quality, cost and timeline expectations.
Key responsibilities include:

โ€ข Lead study-specific eCOA technology deployment and management strategies for internal stakeholders and externally across functions and service providers

โ€ข Participate and collaborate with key process partners (e.g. Clinical Supplies, Biostatistics, Vendor Management, Procurement) in the sourcing, evaluation and audit/qualification of eCOA vendors

โ€ข Act as the sponsor eCOA SME and project manager for study deployment projects

โ€ข Lead study teams in development of study-specific user requirements specifications documents and user acceptance testing (UAT) protocols and execution. Ensure Good Documentation Practices are followed

โ€ข Provide support to study teams to resolve eCOA issues during the conduct of the study

โ€ข Collaborate with study teams during the protocol development process to understand requirements for eCOA technologies

โ€ข Effectively manage operational delivery with eCOA service providers; collect issues and trends from study teams; proactively work with Vendor Management and eCOA vendors for issue resolution and prevention

โ€ข Collaborate internally and with eCOA service providers to implement standards on both system design and data reporting

โ€ข Ensure the availability and delivery of training programs for relevant internal staff

โ€ข Collaborate with and supports other teams by streamlining data flow between eCOA and other systems (e.g. CTMS, Data Warehouse, Clinical Gateway, Clinical Supplies Management System)

โ€ข Ensure trust through transparency in communication and individual actions; ensure outcomes are organizationally driven rather than individually driven; promote collaborative organizational success

โ€ข Develop strategies to prioritize and deliver eCOA related initiatives in coordination with multiple internal departments

โ€ข Direct activities of eCOA vendors, ensuring compliance with specifications and the oversight of timelines and budgets

โ€ข Coordinate evaluation and impact assessment of changes in the eCOA landscape and makes recommendations for actions

โ€ข Provide support to teams on audit-related issues for eCOA services

โ€ข Ensure audit and inspection observations are evaluated and remediated in conjunction with the study team

Your Profile:


Required qualifications and experience:

  • Bachelor's degree in computer science, information technology, or a related discipline
  • 8+ years of relevant experience in a Clinical Research technology-related role within the Pharmaceutical, CRO, or technology vendor industries
  • Strong knowledge / experience with eCOA/ePRO systems and their function within clinical trials
  • Experience with eConsent/Telehealth/Connected Solutions is preferred for this position
  • Proven leadership skills with the ability to effectively manage cross-functional teams and projects
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with internal and external stakeholders
  • Detail-oriented with strong analytical and problem-solving abilities
  • Experience with technology evaluation, deployment, and project management
  • Willingness to travel as required (approximately 15%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requestย here.

Are you a current ICON Employee? Please click here to apply